天津医药 ›› 2017, Vol. 45 ›› Issue (6): 593-595.doi: 10.11958/20170078

• 实验研究 • 上一篇    下一篇

大黄酚对脑缺血/再灌注小鼠脑组织 NO 的影响和 断头抗缺氧作用

王四海 1,梁春利 1,张海红 2,王树 2△   

  1. 1 河北北方学院第二附属医院心胸外科(邮编 075100);2 河北北方学院药学系
  • 收稿日期:2017-01-18 修回日期:2017-05-10 出版日期:2017-06-15 发布日期:2017-07-05
  • 通讯作者: △通讯作者 E-mail:wangshu388@163.com E-mail:wangshu388@163.com
  • 作者简介:王四海(1970),男,硕士研究生,副主任医师,主要从事多器官损伤保护研究
  • 基金资助:
    河北省科技支撑计划项目(07276166);河北北方学院自然科学研究项目(2010022)

Effects of chrysophanol on NO of brain tissue and anti-anoxia in mice with cerebral ischemia-reperfusion injury

WANG Si-hai1, LIANG Chun-li1, ZHANG Hai-hong2, WANG Shu2△   

  1. 1 Department of Cardiothoracic Surgery, the Second Affiliated Hospital of Hebei North University, Xuanhua 075100, China; 2 Department of Pharmacy, Hebei North University
  • Received:2017-01-18 Revised:2017-05-10 Published:2017-06-15 Online:2017-07-05
  • Contact: △Corresponding Author E-mail: wangshu388@163.com E-mail:wangshu388@163.com

摘要: 目的 研究大黄酚(Chry)对小鼠脑缺血/再灌注损伤后脑组织内 NO 的影响及其断头抗缺氧作用。方 法 将 75 只 SPF 级昆明种小鼠随机分为假手术组、模型组、大黄酚高剂量组(Chry 10.0 mg/kg)、中剂量组(Chry 1.0 mg/kg)、低剂量组(Chry 0.1 mg/kg)。采用改良 Himori 法制作小鼠脑缺血/再灌注损伤模型,根据 Bederson 评分标准 测定小鼠神经功能损伤评分。对各组小鼠进行断头抗缺氧实验,记录小鼠喘息时间,并测定脑组织内 NO 的含量。 结果 与模型组比较,大黄酚低、中、高剂量组脑缺血再灌注后神经功能损伤评分和脑组织 NO 含量明显降低,断头 抗缺氧的喘息时间(s)明显延长[低剂量组,14.6±1.2;中剂量组,16.4±1.2;高剂量组,17.4±1.1;与模型组(13.2±1.0)比 较,均 P<0.05]。结论 大黄酚可通过减少脑内 NO 含量和抗缺氧作用对脑缺血/再灌注损伤起到保护效应。

关键词: 大黄酚, 脑缺血, 再灌注损伤, 一氧化氮, 抗缺氧, Himori 法

Abstract: Objective To study the effects of chrysophanol(Chry)on NO of brain tissue and anti-anoxia in mice with cerebral ischemia-reperfusion injury. Methods A total of 75 SPF Kunming mice were randomly allocated into five groups: sham operation group, ischemia-reperfusion group, high-dose group (Chry 10.0 mg·kg- 1), medium-dose group (Chry 1.0 mg · kg- 1) and low-dose group (Chry 0.1 mg·kg- 1). Using improved Himori method, cerebral ischemia reperfusion-injury model was produced in conscious mice by temporarily obstructing bilateral common carotid arteries. The neurological function was measured according to the Bederson scoring standard. The mice were subjected to decapitation for hypoxia tolerance test. The gasping time was measured by anoxia tolerance test in beheaded mice. The level of NO in cerebrum was detected. Results Chrysophanol can decrease the level of NO in cerebrum of mice with cerebral ischemia- reperfusion injury and prolong the gasping time in beheaded mice with cerebral ischemia-reperfusion injury [low-dose group, (14.6±1.2) s; medium- dose group, (16.4 ± 1.2)s; high- dose group, (17.4 ± 1.1)s; ischemia-reperfusion group, (13.2 ± 1.0)s, P<0.05]. Conclusion The protective effects of chrysophanol on cerebral ischemia-reperfusion injury are involved in decreasing the content of NO in brain tissue and anti-anoxia in mice.

Key words: Chrysophanol, brain ischemia, reperfusion injury, nitric oxide, anti-anoxia, Himori method